FDA Inspection 703143 — DGH Technology Inc

DGH Technology Inc — FEI 2522950

The FDA completed an inspection of DGH Technology Inc on Dec 22, 2010 in Exton, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 22, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Exton, PA (United States)